# K993364: GE Logiq 700 with Coded Excitation Modification

- Pathway: 510(k) (Special)
- Applicant: Ge Medical Systems, Inc.
- Decided: Nov 5, 1999 after 30 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K930768 (1994). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K930768: Orion Diagnostic Ultrasound System, GE Medical Systems (1994) Summary page 1.
- K960527: Logiq 1000 Diagnostic Ultrsound System, GE Medical Systems (1997) Summary page 1.
- K964617: GE Logiq 700 Diagnostic Ultrasound System, GE Medical Systems (1997) Summary page 1.
- K964886: GE Logiq 700 Diagnostic Ultrasound System, GE Medical Systems (1997) Summary page 1.
- K990226: GE LOGIQ700 Diagnostic Ultrasound System with B-Flow, Ge Medical Systems, Inc. (1999) Summary page 1.

## Indications for use
The GE LOGIQ 700 with CE is a general purpose ultrasound imaging system intended for use in the evaluation of soft tissue and vascular disease in the head, neck, chest, abdomen, pelvis, male and female reproductive organs, limbs and pregnant uterus. Specific indications are: fetal, abdominal; intraoperative abdominal and neurological; pediatric; small organ including breast, testes, thyroid; neonatal cephalic; cardiac adult and pediatric; TR; TV; PV; urological, and conventional and superficial musculo-skeletal.

Source page: https://510kreport.com/device/K993364
Methodology: https://510kreport.com/methodology